Find & Apply For Quality Control Analyst Jobs in Buena Park, California

Quality Control Inspector Production GuruNanda LLC Buena Park, CA Job Details Full-time $25 - $30 an hour 1 hour ago Benefits Health insurance Dental insurance 401(k) Vision insurance Life insurance Qualifications Quality control experience within consumer goods industry Computer operation Pharmaceutical regulatory compliance Computer literacy Basic math English Manufacturing facility experience Quality control experience within pharmaceutical industry Production batch record review FDA regulations Pharmaceutical manufacturing facility experience

Full Job Description Position Summary:

We are seeking a knowledgeable and hands-on QC Inspector to oversee Quality activities on the production floor, ensuring real-time compliance with FDA regulations (21 CFR Parts 111, 210, and 211), cosmetic GMPs, and internal SOPs. The ideal candidate brings strong experience in-process QC, documentation control and line clearances within the manufacturing of cosmetics, OTC drugs, dietary supplements, and potentially medical devices.

Key Responsibilities:

To issue the FG master, Fill & Assembly Spec and production forms to the production lead. To conduct line clearance for packaging and compounding. To inspect the product during production to make sure the product meets the specifications and documentation is complete. Complete batch records in a timely manner to ensure accuracy and compliance To review and approve First article. To conduct the AQL on the finished product pallet. To collect the Micro, Retain and Assay samples and give it to QC lab. To review the GMP compliance in production, compounding and warehouse area. To conduct the daily verification of scales. Assisting QC leads in preparing and updating the FG Master. Monitor the DI water system and test the quality of water. Report any unusual quality incident to immediate supervisor in a timely manner. To identify & control the nonconforming product and complete the non-conformance report. Assist in root cause investigations and CAPAs implementation for production-related non-conformances. Collaborate closely with Production, Warehouse & QA teams to resolve real-time quality issues Other duties and responsibilities as required by Management.

Qualifications:

Minimum 2-3 years of progressive experience in Quality Control and/or Assurance within OTC Drug and Dietary Supplement manufacturing Experience with cGMP, line clearance, in-process QC, AQL sampling plan and batch record completion. Ability to lead by example and drive quality culture on the production floor Speak and write English Basic mathematics skills Basic computer skills Responsibilities may be shifted based on the department and company's demand Flexibility in work schedule

Pay:

$25.00 - $30.00 per hour

Benefits:

401(k) Dental insurance Health insurance Life insurance Vision insurance Application Question(s): How many years of hands-on QC experience do you have in OTC drug or dietary supplement manufacturing, and what products have you worked with? Can you walk me through how you perform a line clearance for a packaging or compounding operation before production begins? What hands-on experience do you have performing in-process inspections and AQL sampling of finished products? What are you checking for? What experience do you have completing or reviewing batch records and handling a nonconformance when a product does not meet specifications?

Work Location:

In person